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nsv4493594

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 46 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):163,446,457-163,446,457Question Mark
Overlapping variant regions from other studies: 46 SVs from 7 studies. See in: genome view    
Submitted genomic162,873,463-162,873,463Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4493594RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5163,446,457163,446,457
nsv4493594Submitted genomicGRCh37.p13Primary AssemblyNC_000005.9Chr5162,873,463162,873,463

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16065312alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16065312RemappedPerfectNC_000005.10:g.163
446457_163446458in
s281
GRCh38.p12First PassNC_000005.10Chr5163,446,457163,446,457
nssv16065312Submitted genomicNC_000005.9:g.1628
73463_162873464ins
281
GRCh37.p13NC_000005.9Chr5162,873,463162,873,463

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16065312<0.001721692
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